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Administering
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Guidance
Administering
Supply and/or administration of Controlled Drugs under a PGD
16 November 2021
·
The legal position on the supply and/or administration of controlled drugs under Patient Group Directions is summarised
Guidance
Administering
Unlicensed medicines and use of PGDs
16 November 2021
·
This page explains why PGDs are not a legal mechanism for the administration or supply of unlicensed medicines.
Guidance
Administering
Understanding why PGDs cannot be used for dose adjustments
16 November 2021
·
This article outlines why PGDs cannot be used to adjust the dosage of a medicine already in an individual's possession.
Guidance
Administering
Off label medicine use under a Patient Group Direction
10 June 2021
·
This article explains the legislation and guidance on the use of PGDs when a medicine is to be used outside its licence ('off-label').
Guidance
Administering
Legal mechanisms and their application to give COVID-19 vaccines
7 January 2021
·
A summary of the different legal mechanisms available, a priority order for the options, and advice on their application to different professional groups.
Guidance
Administering
All our advice relating to administering medicines; ranging from legal mechanism frameworks through to practical administration.
Guidance
Administering
Abortifacients and Patient Group Directions (PGDs)
14 September 2020
·
This article advises on the legal position on the supply/administration of abortifacients under PGDs.
Guidance
Administering
Mixing of medicines and Patient Group Directions
9 September 2020
·
This article provides advice on the legal considerations required when considering mixing medicines to be supplied or administered under a PGD.
Guidance
Administering
Patient Group Direction use in End of Life Care
10 August 2020
·
Considerations required before implementing Patient Group Directions (PGDs) in End of Life Care.
Guidance
Administering
Off-label or unlicensed product use under HMR 2012 exemptions
8 January 2020
·
A legal position summary regarding the sale, supply or administration of off-label/unlicensed products under Schedule 17 of the Human Medicines Regulations 2012
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